Job Details
Role: Associate Pharmacovigilance Specialist
Department: Life Sciences & Healthcare
Work Mode: Hybrid
Locations: Available in 2 locations
Job ID: JREQ134094
Posted On: October 28th, 2025
Working Hours: 12:00 PM – 9:00 PM (Regular)
Role Summary
The Associate Pharmacovigilance Specialist is responsible for performing pharmacovigilance activities such as biomedical literature monitoring, identifying adverse event information, and completing indexing and abstracting tasks. This role involves applying strong knowledge of scientific terminology, medical concepts, drug safety regulations, and therapeutic areas.
Key Responsibilities
Screen biomedical literature to identify safety information related to pharmaceutical products.
Assess identified adverse events and ensure all reportable cases comply with pharmacovigilance regulatory requirements.
Conduct regular literature reviews to capture potential adverse events.
Summarize relevant scientific information from case reports, studies, and biomedical publications.
Required Qualifications
Education
Master’s degree in Life Sciences, Health, or Biomedical Sciences (e.g., Pharmacy, Microbiology, Biochemistry, Biotechnology, Biophysics).
Experience
Freshers or up to 2 years of experience in reviewing biomedical literature for AE reporting.
OR equivalent combination of education and experience (e.g., Information Science degree + 1 year relevant experience).
Experience in drug safety/pharmacovigilance is desirable.
Skills
Strong analytical ability to interpret and summarize biomedical case reports and literature.
Good knowledge of biomedical and medical terminology.
Understanding of drugs, therapeutic areas, and pharmacovigilance regulations.
Familiarity with commercial and client-specific biomedical literature databases.
Preferred / Added Advantages
Certification from a professional medical writers association.
Medical/scientific writing experience.
Experience working with biomedical literature databases.
Degree in Dentistry, Physiotherapy, or Nursing (advantage due to clinical/patient exposure).
About the Team
The Pharmacovigilance team consists of professionals across India, each reporting to their respective team managers. The team brings combined expertise in market research, consulting, and healthcare, especially in the medical devices and pharmaceutical sectors.
Company Statement
Clarivate is committed to providing equal employment opportunities in hiring, compensation, promotion, training, and all employment practices. All policies comply with applicable non-discrimination laws and regulations.
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